Top 2272 Oncology program coordinator Jobs

Clinical Research Coordinator
Mission Cancer + Blood, part of University of Iowa Health Care —Waukee, IA
- Full-time
- Background check
- Nursing
- RN License
- Health insurance
- Dental insurance
Quick Apply
11d
Clinical Research Coordinator
Actalent —Palo Alto, CA
- $30 - $31 an hour
- Contract
- Vital signs
- Ability to walk for extended periods
- Mid-level
- Commuter assistance
- Health savings account
Quick Apply
8d
Oncology Program Access Coordinator
Cancer Center of South Florida PLLC —West Palm Beach, FL
- Call employer
- HIPAA
- Mid-level
- 3 years
Quick Apply
Patient Services Coordinator - Oncology
Hartford Hospital —Hartford, CT
- Full-time
- 5 years
- Mid-level
- Children
Quick Apply
Team Lead, Enrollment Quality Assurance
Thyme Care —Remote
- $80,000 a year
- Full-time
- Remote
- 5 years
- Mid-level
- Supervising experience
Quick Apply
8d
Clinical Research Coordinator
START Center for Cancer Research —East Brunswick, NJ
- Monday to Friday
- Mid-level
- High school diploma or GED
- Travel
- Health savings account
- Paid holidays
Quick Apply
12h
Patient Services Coordinator - Oncology (Per Diem)
Hartford Hospital —Manchester, CT
- Monday to Friday
- 5 years
- High school diploma or GED
- Children
Quick Apply
CANCER PROGRAM COORDINATOR
Calvert Health System —Prince Frederick, MD
- $33.00 - $44.50 an hour
- Full-time
- Nursing
- Microsoft Access
- Microsoft Outlook
Quick Apply
Patient Service Coordinator - Oncology
St. Vincent's Medical Center —Fairfield, CT
- Full-time
- High school diploma or GED
- Children
- Travel
Quick Apply
Oncology Access Coordinator
George Washington Medical Faculty Associates —Washington, DC
- $21.44 - $25.48 an hour
- Microsoft Excel
- Mid-level
- Office
Quick Apply
Office Coordinator - Oncology
The Hospital of Central Connecticut —New Britain, CT
- Full-time
- Mid-level
- High school diploma or GED
- Children
Quick Apply
11d
RN - Registered Nurse Coordinator - Transplant
Geisinger —Danville, PA
- Full-time
- Nursing
- Vital signs
- Surgery
- Wellness program
- Health savings account
Registered Nurse, Home Health
AccentCare —Mechanicsburg, PA
- $87,000 - $100,000 a year
- Full-time
- Management
- RN License
- Mid-level
- Wellness program
- Mileage reimbursement
Clinical Nurse Coordinator CVICU
Corpus Christi Medical Center The Heart Hospital —Corpus Christi, TX
- Full-time
- Psychiatry
- Mid-level
- Radiology
- Employee stock purchase plan
- Disability insurance
Quick Apply
11d
Registered Nurse - Home Health - Weekends
Accentcare —Marysville, PA
- $87,000 - $100,000 a year
- Full-time
- Management
- RN License
- Mid-level
- Health savings account
- Paid holidays
Clinical Research Principal Investigator
Vitaly Clinical Research —Plano, TX
- From $120,000 a year
- Contract
- Medicine
- Psychiatry
- BC/BE
- Flexible schedule
Quick Apply
11d
RN - Registered Nurse - Performance Improvement Coordinator
Geisinger —Wilkes-Barre, PA
- Full-time
- Nursing
- RN License
- Hospital
- Wellness program
- Health savings account
Research Pharmacist (Per Diem - Investigational Drug Service)
Folio Clinical Research —Bakersfield, CA
- $75 - $110 an hour
- Part-time
- Mid-level
- Clinic
- Patient care
Quick Apply
Assistant Director of Nursing
Caris HealthCare —Nashville, TN
- $81,000 - $90,000 a year
- Nursing
- Management
- RN License
- Paid training
- Mileage reimbursement
Quick Apply
Cancer Nurse Navigator
Renown Health —Reno, NV
- Full-time
- Nursing
- Microsoft Excel
- Microsoft Outlook

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Clinical Research Coordinator

Mission Cancer + Blood, part of University of Iowa Health Care -
Waukee, IA

Quick Apply

Job Details

Full-time
11 days ago

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Life insurance
Retirement plan

Qualifications

Clinical research
RN License
Employee relationship building
Clinical trials
CCRP

Full Job Description

Position Title: Clinical Research Coordinator

Summary: This position is responsible for organizing, planning and controlling work flow of all clinical research related activities. The Clinical Research Coordinator is required to have an in-depth knowledge of clinical trial requirements and good clinical practices as set forth by federal regulations. As the primary resource for the clinical trials, the coordinator will act as liaison between the investigators, the institutional review board (IRB), and the study sponsors. Along with the investigator, the research coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the research coordinator will be responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory files.

Essential Duties and Responsibilities include the following. Other duties may be assigned.

Communications / Liaison:

Maintain cooperative relationship with co-workers, component hospital departmental staff, investigator medical office staff, study sponsor contacts, and clinical research participants.
Answer telephone, screen calls, take messages, and provide information to appropriate staff.
Communicate on a regular basis with investigators and office nurses regarding the availability of clinical studies.
Act as liaison between investigators and study sponsor staff.
Maintain cooperative relationship with co-workers, component hospital departmental staff, investigator medical office staff, study sponsor contacts, and clinical research participants.
Attend component hospital Tumor Board conferences when assigned.
Communicate needs for laboratory, pathology, and/or radiology submissions.
Communicate investigational drug orders and schedules to designated pharmacist.

Screening and Enrollment:

Ascertain that there is documented IRB approval to the IRB for clinical trials prior to registration/randomization
Review the study design and inclusion/exclusion criteria with the investigator.
Review and verify all relevant source documentation in the subject's medical record to confirm study eligibility. Review the protocol, informed consent form, and follow-up procedures with potential study subjects if so directed by the investigator.
Ensure the current approved informed consent and HIPAA agreement form are signed before subjects are screened and enrolled.
Ensure that the registration/randomization procedure is followed as per protocol guidelines.
Document record of the subject's registration/randomization as well as data assigned and/or waived by the registering study sponsor.
Maintain accrual log and spreadsheet of protocol patients.
Enter registered/randomized subjects into database.
Calculate and verify protocol treatment drug dosages with a second CRA and the treating investigator.

Subject Follow-up:

Prepare, maintain, and distribute a subject calendar with treatment schedule, test schedule, and follow-up schedule to ensure adherence to protocol requirements.
Monitor dosage modifications and treatment calculations.
Obtain continuous follow-up information on subject's medical status per protocol.
Assess and record all adverse drug events as outlined in the protocol.
Report adverse drug events / attribution according to federal and study sponsor guidelines by completing required forms and online data submission.
Ensure appropriate specimen collection as required per protocol.

Data Management:

Collate data for submission to meet protocol requirements.
Abstract data from appropriate sources to complete case report forms.
Key data for remote data entry or submit completed case report forms per protocol guidelines.
Maintain source documentation for all case report form entries, including clinic chart visit notes, lab data, radiology reports, pathology reports, operative reports, and hospitalizations.
Ensure resolution of study sponsor queries in timely manner.
Review study sponsor delinquency reports for deficiencies.
Correct and edit case report forms, as appropriate.

Other:

Assist in training of all new CRAs, chemotherapy nurses, and investigator assigned nurses.
Assist Pharmacist in ordering investigational drugs, maintaining drug accountability records, and delivery of investigational drugs to satellite offices.
Assist in internal quality assurance program and routine monitoring audits.
Participate in presentations or seminars related to the field of clinical research.

Supervisory Responsibilities

This job has no supervisory responsibilities.

Qualifications:

Education and/or Experience:

Certified Clinical Research Professional, Registered Nurse, or B.S. in Health Related Field. Equivalent related work experience can be substituted for educational experience. Oncology and/or clinical research experience preferred. Computer experience in Database software, Internet software and Word Processing software preferred.
Frequent travel to local satellite offices is required. Occasional overnight travel to sponsor meetings is also required for training purposes and updates.

Job Type: Full-time

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Retirement plan

Work Location: In person

Quick Apply

Refine Your Search

oncology program coordinator jobs

Clinical Research Coordinator

Clinical Research Coordinator

Oncology Program Access Coordinator

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Clinical Research Coordinator

Patient Services Coordinator - Oncology (Per Diem)

CANCER PROGRAM COORDINATOR

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Oncology Access Coordinator

Office Coordinator - Oncology

RN - Registered Nurse Coordinator - Transplant

Registered Nurse, Home Health

Clinical Nurse Coordinator CVICU

Registered Nurse - Home Health - Weekends

Clinical Research Principal Investigator

RN - Registered Nurse - Performance Improvement Coordinator

Research Pharmacist (Per Diem - Investigational Drug Service)

Assistant Director of Nursing

Cancer Nurse Navigator

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